3-Chloro-4-ethoxyphenylboronic Acid (contains varying amounts of Anhydride)

98%

Reagent Code: #90208
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CAS Number 279261-81-3

science Other reagents with same CAS 279261-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.43 g/mol
Formula C₈H₁₀BClO₃
badge Registry Numbers
MDL Number MFCD03701556
thermostat Physical Properties
Melting Point 234-239°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of biologically active compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This chemical is also employed in the development of agrochemicals, contributing to the creation of herbicides and pesticides. Its boronic acid group makes it valuable in organic synthesis and material science, where it aids in the preparation of advanced polymers and functional materials. Additionally, it is utilized in research and development for designing new drug candidates and studying enzyme inhibitors.

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Test Parameter Specification
Purity 97.5-100
Appearance White to light yellow crystalline powder

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,314.00

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3-Chloro-4-ethoxyphenylboronic Acid (contains varying amounts of Anhydride)
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of biologically active compounds. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This chemical is also employed in the development of agrochemicals, contributing to the creation of herbicides and pesticides. Its boronic acid group makes it valuable in organic synthesis and material science, where it aids in the preparation of advanced polymers and functional materials. Additionally, it is utilized in research and development for designing new drug candidates and studying enzyme inhibitors.
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